Our Patient Community

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• At Consultation Club, patients are at the heart of everything we do. We believe that access to clinical research should be clear, compassionate, and empowering. Whether you are exploring clinical trial participation for the first time or looking for support in understanding your options, our team is here to guide you every step of the way.
• Clinical trials offer patients the opportunity to access innovative therapies while contributing to medical advancements that benefit people around the world. 
• Our mission is to create a safe, respectful, and supportive environment where you can make informed decisions about your health.

Participating in a clinical study can offer:                  

• Access to New Treatments
  Potential to receive therapies not yet available to the public.
   
• Expert Medical Oversight
  Close monitoring by experienced physicians, nurses, and clinical research professionals.
   
• Contribution to Medical Progress
  Your participation helps advance the understanding of diseases and leads to better treatments for future generations.
   
• No Cost to You
  Study-related visits, tests, and treatments are typically provided at no cost.
   

Your health, safety, and well-being remain the top priority throughout the entire process!                         

We are committed to ensuring your experience is:                                                                                               

• Safe: We follow strict international standards (ICH-GCP), regulatory requirements, and ethical guidelines to protect your rights and safety at all times.
• Informed: You will receive clear, transparent information about the study, including its details, risks, benefits, and your rights as a participant.
• Voluntary: Participation is entirely voluntary, and you may withdraw at any time without affecting your medical care.
• Supported: Our team is here to answer your questions, explain the process, and ensure you feel comfortable and respected throughout your journey!

The research process typically involves:                      

• Pre-Screening: We ask a few simple questions to determine whether a study may be a good match for you.
• In-Clinic Screening Visit: A detailed health review, medical history, and study-specific assessments are performed to ensure the trial is appropriate and safe for you.
• Informed Consent: You will be given clear, written information describing the trial. A study team member will explain it in detail and answer all your questions before you sign.
• Study Participation: You attend scheduled visits, receive study-related care, and remain in close communication with the research team.
• Follow-Up: Some studies include short- or long-term follow-up visits to check on your health and collect additional information!

As a participant in a trial, you have the rights:                                                                 

• To receive comprehensive information about the study. 
• To ask questions at any time. 
• To decline participation or withdraw from the study at any point. 
• To have your personal information protected.
• To receive medical care and oversight related to the study.  

Your dignity, safety, and privacy will always be respected.                                                                              

Studies have specific eligibility criteria based on:                                                                     

• Age
• Medical condition
• Treatment history
• Current medications
• Overall health status

If you are unsure whether you qualify, our team can help you determine which studies may be right for you.